Dawa, T., Farrington, J. (2008). Conflict between nomadic herders and brown bears in the Byang thang Region of Tibet. Journal of the International Association of Tibetan Studies, 4(December), 1–42.
Abstract: Article covers the human-brown bear conflict problem, which closely parallels that of snow leopard conflict in the TAR, the peer reviewed version of: Tsering, Dawa, John D. Farrington, and Kelsang Norbu. Competition and Coexistence: Human-Wildlife Conflict in the Chang Tang Region of Tibet. Lhasa, Tibet Autonomous Region, China: Tibet People’s Publishing House, 2007.
In order to evaluate the impact of recently introduced wildlife conservation policies, a human-wildlife conflict survey of three-hundred herding households was conducted in the south-central Byang thang (Qiangtang) area of the Tibet Autonomous Region (bod rang skyongs ljongs, Xizang Zizhi Qu). Results showed that Tibetan brown bears were the largest source of human-wildlife conflict in the survey area, affecting 49 percent of surveyed households between 1990 and 2006, with a 4.5-fold increase in conflict with bears occurring since implementation of various wildlife protection policies beginning in 1993. Types of bear conflict included livestock kills, raiding of human food supplies, damage to dwellings and furnishings, and direct attacks on herders. Brown bears have caused devastating
economic losses to herders and anecdotal evidence indicates that retaliatory killing of bears by herders now poses the greatest threat to the Tibetan brown bear. Immediate measures must be taken to resolve this conflict if humans and brown
bears are to coexist in the Byang thang region.
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Gee, E. P. (1967). Occurrence of the snow leopard Panthera uncia (Schreber) in Bhutan. Journal of the Natural History Museum Society, 30, 634–636.
Abstract: Indicates that snow leopard range includes all of Northern Bhutan
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Vipin, G., T. R., Sharma, V., Kumar, B. K., Gaur, A. (2022). Kleptoparasitic interaction between Snow Leopard Panthera uncia and Red Fox Vulpes vulpes suggested by circumstantial evidence in Pin Valley National Park, India. Journal of Threatened Taxa, 14(10), 21928–21935.
Abstract: In the present study, we describe an interspecific kleptoparasitic interaction between two sympatric mammalian carnivores in the high altitudinal Trans-Himalaya region of Himachal Pradesh, India. The study was based on the inferences drawn from the circumstantial evidence (direct and indirect) noticed in the study area in Pin Valley National Park. The inferences from the analysis of the evidence suggested the interaction between a Snow Leopard Panthera uncia, a Red Fox Vulpes vulpes, and a donkey. The arrangement of evidence in a sequential manner suggested that a donkey was killed by a Snow Leopard and a Red Fox stole the food from the carrion of the Snow Leopard’s prey. The Red Fox was killed by the Snow Leopard, which was caught while stealing. The present study represents an example of kleptoparasitic interaction between the Snow Leopard and the Red Fox. This study also proves that such interactions may cost the life of a kleptoparasite and supports the retaliation behaviour of Snow Leopards.
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Ale, S., Shrestha, B., and Jackson, R. (2014). On the status of Snow Leopard Panthera Uncia (Schreber 1775) in Annapurna, Nepal. Journal of Threatened Taxa, (6(3)), 5534–5543.
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Lama, R. P., Ghale, T. R., Suwal, M. K., Ranabhat, R., Regmi, G. R. (2018). First photographic evidence of Snow Leopard Panthera uncia (Mammalia: Carnivora: Felidae) outside current protected areas network in Nepal Himalaya. Journal of Threatened Taxa, , 12086–12090.
Abstract: The Snow Leopard Panthera uncia is a rare top predator of high-altitude ecosystems and insufficiently surveyed outside of protected areas in Nepal. We conducted a rapid camera-trapping survey to assess the presence of Snow Leopard in the Limi valley of Humla District. Three individuals were recorded in two camera locations offering the first photographic evidence of this elusive cat outside the protected area network of Nepal. In addition to Snow Leopard, the Blue Sheep Pseudois nayaur, Beech Marten Martes foina, Pika Ochotona spp. and different species of birds were also detected by camera-traps. More extensive surveys and monitoring are needed for reliably estimating the population size of Snow Leopard in the area. The most urgent needs are community-based conservation activities aimed at mitigating immediate threats of poaching, retaliatory killing, and rapid prey depletion to ensure the survival of this top predator in the Himalaya.
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Shrestha, A., Thapa, K., Subba, S. A., Dhakal, M., Devkota, B. P., Thapa, G. J., Shrestha, S., Malla, S., Thapa, K. (2019). Cats, canines, and coexistence: dietary differentiation between the sympatric Snow Leopard and Grey Wolf in the western landscape of Nepal Himalaya. Journal of Threatened Taxa, 11(7), 13815–13821.
Abstract: Understanding the dietary habits of sympatric apex carnivores advances our knowledge of ecological processes and aids their conservation. We compared the diets of the sympatric Snow Leopard Panthera uncia and Grey Wolf Canis lupus using standard micro-histological analyses of scats collected from the western complex of Nepal Himalaya. Our study revealed one of the highest recorded contributions of livestock to the diet of top predators (55% for Grey Wolf and 39% for Snow Leopard) and high dietary overlap (0.82) indicating potential exploitative or interference competition. Their diet composition, however, varied significantly based on their consumption of wild and domestic prey. Limitation in data precludes predicting direction and outcome of inter-specific interactions between these predators. Our findings suggest a high rate of negative interaction with humans in the region and plausibly retaliatory killings of these imperilled predators. To ensure the sustained survival of these two apex carnivores, conservation measures should enhance populations of their wild prey species while reducing livestock losses of the local community through preventive and mitigative interventions.
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Helman, R. G., Russell, W. C., Jenny, A., Miller, J., & Payeur, J. (1998). Diagnosis of tuberculosis in two snow leopards using polymerase chain reaction (Vol. 10).
Abstract: The incidence of tuberculosis in zoological animal collections is low, and the disease is monitored through skin testing primarily in primates and artiodactylids.15,16 Other exotic animals are clearly at risk; tuberculosis has been described in elephants (Mycobacterium tuberculosis, M. bovis), rhinoceros (M. bovis), felids (M. bovis), foxes (M. bovis), birds (M. avium complex, M. tuberculosis, M. bovis), and reptiles, amphibians, and fish (cryophilic Mycobacterium species). 1,2,4,6,8-10,13,14,17 Mycobacterial infections in mammals and birds serve as a potential source of disease that can spread to other animals and to humans.7,15,16 In humans, M. bovis and M. tuberculosis are the most important mycobacteria in the USA.
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McCarthy, K., Fuller, T., Ming, M., McCarthy, T., Waits, L., & Jumabaev, K. (2008). Assessing Estimators of Snow Leopard Abundance (Vol. 72).
Abstract: The secretive nature of snow leopards (Uncia uncia) makes them difficult to monitor, yet conservation efforts require accurate and precise methods to estimate abundance. We assessed accuracy of Snow Leopard Information Management System (SLIMS) sign surveys by comparing them with 4 methods for estimating snow leopard abundance: predator:prey biomass ratios, capture-recapture density estimation, photo-capture rate, and individual identification through genetic analysis. We recorded snow leopard sign during standardized surveys in the SaryChat Zapovednik, the Jangart hunting reserve, and the Tomur Strictly Protected Area, in the Tien Shan Mountains of Kyrgyzstan and China. During June-December 2005, adjusted sign averaged 46.3 (SaryChat), 94.6 (Jangart), and 150.8 (Tomur) occurrences/km. We used
counts of ibex (Capra ibex) and argali (Ovis ammon) to estimate available prey biomass and subsequent potential snow leopard densities of 8.7 (SaryChat), 1.0 (Jangart), and 1.1 (Tomur) snow leopards/100 km2. Photo capture-recapture density estimates were 0.15 (n = 1 identified individual/1 photo), 0.87 (n = 4/13), and 0.74 (n = 5/6) individuals/100 km2 in SaryChat, Jangart, and Tomur, respectively. Photo-capture rates
(photos/100 trap-nights) were 0.09 (SaryChat), 0.93 (Jangart), and 2.37 (Tomur). Genetic analysis of snow leopard fecal samples provided minimum population sizes of 3 (SaryChat), 5 (Jangart), and 9 (Tomur) snow leopards. These results suggest SLIMS sign surveys may be affected by observer bias and environmental variance. However, when such bias and variation are accounted for, sign surveys indicate relative abundances similar to photo rates and genetic individual identification results. Density or abundance estimates based on capture-recapture or ungulate biomass did not agree with other indices of abundance. Confidence in estimated densities, or even detection of significant changes in abundance of snow leopard, will require more effort and better documentation.
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Peden, W. M., Richard, J. L., Trampel, D. W., & Brannian, R. E. (1985). Mycotic pneumonia and meningoencephalitis due to Aspergillus terreus in a neonatal snow leopard (Panthera uncia) (Vol. 21).
Abstract: On 14 May 1983, two female snow leopard (Panthera uncia) cubs were born in the Kansas City Zoological Gardens to a primiparous female. The female showed little interest in the cubs, one of which had a body temperature of 30 C, so they were removed for hand-rearing. On 15 May, one cub was less active, and did not nurse as well as its littermate.
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Oli, M. K., & Rogers, E. M. (1996). Seasonal pattern in group size and population composition of blue sheep in Manang, Nepal. Journal of Wildlife Management, 60(4), 797–801.
Abstract: Blue sheep (Pseudois nayaur) are the principal prey of the endangered snow leopard (Panthera uncia) in the Himalayas and adjacent ranges. We studied group size and population composition of blue sheep in Manang District, Annapurna Conservation Area, Nepal. Overall mean group size was 15.6 (SE = 1.3), but it varied seasonally (P lt 0.001), with significantly smaller groups in winter than in other seasons. Mixed groups were most numerous in all seasons, and there was no evidence of sexual segregation. Yearling sex ratio (93.7 M:100 F) did not vary seasonally, nor did the ratio deviate from parity. Adult sex ratio showed a seasonal pattern favoring males post-parturition but female-biased during the rut and pre-parturition. Seasonal variation in sex-specific mortality is offered as a plausible explanation for the observed pattern in adult sex ratio.
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